Bravos Afterloader System

FDA UDI

Class II (US FDA UDI)

by Varian Medical Systems Deutschland GmbH

Identity

Trade Name: Bravos Afterloader System FDA UDI
Generic Name: Remote-afterloading brachytherapy system FDA UDI
Device Name: Bravos Afterloader System FDA UDI
Model / Reference: VG15000500 FDA UDI
Description: Bravos Afterloader System FDA UDI

Identifiers

Catalog Number: VG15000500 FDA UDI
Primary DI / UDI-DI: 00816389027947 FDA UDI
510(k) Number: K181903 FDA UDI
FDA Product Code: JAQ FDA UDI
GMDN Term: Remote-afterloading brachytherapy system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 892.5700 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Remote-afterloading brachytherapy system

Bravos Afterloader System by Varian Medical Systems Deutschland GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Remote-afterloading brachytherapy system.

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Cleared under the same submission

K181903 also covers:

Transfer Guide Tube for 500 mm catheters — Varian Medical Systems Deutschland GmbH

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Varian Medical Systems Deutschland GmbH

Sources (1)

FDA UDI 90ec880d-b68e-4a25-81e9-4b83ab86adfd 35 fields · synced May 30, 2026